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September 28, 2025The Journal of Physical Chemistry C2 citations

Opposite Charge Transfer to Cocatalyst Surface in SrTiO3:Rh,Sb Photocatalyst for Water Splitting Depending on Excitation Wavelength Observed by In Situ Soft X-ray Absorption Spectroscopy

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KEKota EnomotoRTRyo ToyoshimaZWZi Wang

Key Points

  • Photocatalytic water splitting activity is influenced by the excitation-light energy, changing charge carriers.
  • When using UV light, holes are transferred to the CoOOH cocatalyst, while electrons are transferred under visible light.
  • In situ soft X-ray absorption spectroscopy tracked chemical-state evolution during charge transfers.
  • Understanding this charge transfer mechanism may enhance photocatalytic efficiency for water splitting.

Abstract

A crucial process in photocatalytic water splitting (PWS) is photoinduced charge transfer to reaction sites. Employing surface-sensitive in situ soft X-ray absorption spectroscopy, we measured the chemical-state evolution in Co under working conditions to track the electron and hole transfer to the CoOOH cocatalyst, which works as the oxygen evolution reaction site in Rh/Cr2O3–CoOOH/SrTiO3:Rh,Sb photocatalyst system. We found that the type of charge carrier transferred to the CoOOH cocatalyst is switched by the excitation-light energy; holes for UV light and electrons for visible light. Remarkably, the photocatalytic activity disappears under visible light irradiation, although the visible light photons are readily absorbed by the photocatalyst. We propose a possible scheme of charge transfer and consumption processes that is likely related to the PWS activity. This study highlights the pivotal role of excitation-light energy in charge transfer during the PWS.

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Cite This Study

Enomoto et al. (2025) studied this question.

synapsesocial.com/papers/68d913b74ddcf71ba560c2cehttps://doi.org/10.1021/acs.jpcc.5c05176
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